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Analysis of the local organization and dynamics of cellular actin networks
A ctin filaments, with the aid of multiple accessory proteins, self-assemble into a variety of network patterns. We studied the organization and dynamics of the actin network in nonadhesive regions of cells bridging fibronectin-coated adhesive strips. The network was formed by actin nodes associated...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787384/ https://www.ncbi.nlm.nih.gov/pubmed/24081490 http://dx.doi.org/10.1083/jcb.201210123 |
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author | Luo, Weiwei Yu, Cheng-han Lieu, Zi Zhao Allard, Jun Mogilner, Alex Sheetz, Michael P. Bershadsky, Alexander D. |
author_facet | Luo, Weiwei Yu, Cheng-han Lieu, Zi Zhao Allard, Jun Mogilner, Alex Sheetz, Michael P. Bershadsky, Alexander D. |
author_sort | Luo, Weiwei |
collection | PubMed |
description | A ctin filaments, with the aid of multiple accessory proteins, self-assemble into a variety of network patterns. We studied the organization and dynamics of the actin network in nonadhesive regions of cells bridging fibronectin-coated adhesive strips. The network was formed by actin nodes associated with and linked by myosin II and containing the formin disheveled-associated activator of morphogenesis 1 (DAAM1) and the cross-linker filamin A (FlnA). After Latrunculin A (LatA) addition, actin nodes appeared to be more prominent and demonstrated drift-diffusion motion. Superresolution microscopy revealed that, in untreated cells, DAAM1 formed patches with a similar spatial arrangement to the actin nodes. Node movement (diffusion coefficient and velocity) in LatA-treated cells was dependent on the level and activity of myosin IIA, DAAM1, and FlnA. Based on our results, we developed a computational model of the dynamic formin-filamin-actin asters that can self-organize into a contractile actomyosin network. We suggest that such networks are critical for connecting distant parts of the cell to maintain the mechanical coherence of the cytoplasm. |
format | Online Article Text |
id | pubmed-3787384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37873842014-03-30 Analysis of the local organization and dynamics of cellular actin networks Luo, Weiwei Yu, Cheng-han Lieu, Zi Zhao Allard, Jun Mogilner, Alex Sheetz, Michael P. Bershadsky, Alexander D. J Cell Biol Research Articles A ctin filaments, with the aid of multiple accessory proteins, self-assemble into a variety of network patterns. We studied the organization and dynamics of the actin network in nonadhesive regions of cells bridging fibronectin-coated adhesive strips. The network was formed by actin nodes associated with and linked by myosin II and containing the formin disheveled-associated activator of morphogenesis 1 (DAAM1) and the cross-linker filamin A (FlnA). After Latrunculin A (LatA) addition, actin nodes appeared to be more prominent and demonstrated drift-diffusion motion. Superresolution microscopy revealed that, in untreated cells, DAAM1 formed patches with a similar spatial arrangement to the actin nodes. Node movement (diffusion coefficient and velocity) in LatA-treated cells was dependent on the level and activity of myosin IIA, DAAM1, and FlnA. Based on our results, we developed a computational model of the dynamic formin-filamin-actin asters that can self-organize into a contractile actomyosin network. We suggest that such networks are critical for connecting distant parts of the cell to maintain the mechanical coherence of the cytoplasm. The Rockefeller University Press 2013-09-30 /pmc/articles/PMC3787384/ /pubmed/24081490 http://dx.doi.org/10.1083/jcb.201210123 Text en © 2013 Luo et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Luo, Weiwei Yu, Cheng-han Lieu, Zi Zhao Allard, Jun Mogilner, Alex Sheetz, Michael P. Bershadsky, Alexander D. Analysis of the local organization and dynamics of cellular actin networks |
title | Analysis of the local organization and dynamics of cellular actin networks |
title_full | Analysis of the local organization and dynamics of cellular actin networks |
title_fullStr | Analysis of the local organization and dynamics of cellular actin networks |
title_full_unstemmed | Analysis of the local organization and dynamics of cellular actin networks |
title_short | Analysis of the local organization and dynamics of cellular actin networks |
title_sort | analysis of the local organization and dynamics of cellular actin networks |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787384/ https://www.ncbi.nlm.nih.gov/pubmed/24081490 http://dx.doi.org/10.1083/jcb.201210123 |
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